OMNI Human Resource Management

  • Quality Control Associate

    Job ID
    2018-2255
    Client
    Vince & Associates Clinical Research
    Job Location(s)
    US-KS-Overland Park
  • Overview

    Altasciences- Vince and Asso

    Do you want a fast-paced, exciting and innovative career in research? Vince and Associates Clinical Research is currently looking for a Quality Control Associate for their Overland Park, KS campus.

    Altasciences Clinical Research, encompassing Algorithme Pharma, Vince and Associates Clinical Research and Algorithme Pharma USA, is one of the largest early phase clinical research organizations (CROs) in North America. As a leading, full-service CRO, we have extensive expertise in the execution of a wide range of Phase I/II clinical studies, especially complex trials in healthy normal volunteers and patient populations.

    The Quality Control Associate monitors study activities to ensure compliance with all relevant local, federal, and state regulatory and institutional polices while identifying protocol problems, reviewing study-related documents, and ensuring that appropriate corrections are made and documented for missing or incomplete data. Hours will vary regularly with evening shifts approximately 3PM-11PM with availability on weekdays for day shift training.

     DP-IND

    Responsibilities

    • Monitor study activities to ensure compliance with protocols and compliance with all relevant local, federal, and state regulatory and institutional policies
    • Identify protocol problems, inform investigators of any problems or assist in problem resolution efforts such as protocol revisions
    • Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures
    • Review study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports
    • Ensure appropriate corrections are made and documented for any missing or incomplete data
    • Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review group
    • Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical study affairs and issues

    Qualifications

    • Bachelor’s Degree in the life science related field or equivalent experience
    • 2-3 years Clinical Research experience
    • Ability to interface with busy clinicians and nurses
    • Flexible schedule as hours will vary regularly
    • Demonstrated problem solving and time management skills

    All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, and protected veteran status, or disability status.

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